Ring Troels, Pedersen Birgitte Bang, Salkus Giedrius, Goodship Timothy H J
Department of Nephrology , Aalborg University Hospital , Aalborg , Denmark.
Department of Pathology , Aalborg University Hospital , Aalborg , Denmark.
Clin Kidney J. 2015 Oct;8(5):489-91. doi: 10.1093/ckj/sfv076. Epub 2015 Aug 27.
IgA nephropathy (IgAN) is characterized by a variable clinical course and multifaceted pathophysiology. There is substantial evidence to suggest that complement activation plays a pivotal role in the pathogenesis of the disease. Therefore, complement inhibition using the humanized anti-C5 monoclonal antibody eculizumab could be a rational treatment. We report here a 16-year-old male with the vasculitic form of IgAN who failed to respond to aggressive conventional therapy including high-dose steroids, cyclophosphamide and plasma exchange and who was treated with four weekly doses of 900 mg eculizumab followed by a single dose of 1200 mg. He responded rapidly to this treatment and has had a stable creatinine around 150 µmol/L (1.67 mg/dL) for >6 months. However, proteinuria was unabated on maximal conventional anti-proteinuric treatment, and a repeat renal biopsy 11 months after presentation revealed severe chronic changes. We believe this case provides proof of principle that complement inhibition may be beneficial in IgAN but also that development of chronicity may be independent of complement.
IgA肾病(IgAN)具有临床病程多变和病理生理多方面的特点。有大量证据表明补体激活在该疾病的发病机制中起关键作用。因此,使用人源化抗C5单克隆抗体依库珠单抗抑制补体可能是一种合理的治疗方法。我们在此报告一名16岁男性IgAN血管炎型患者,他对包括大剂量类固醇、环磷酰胺和血浆置换在内的积极常规治疗无反应,接受了4周每周一次900毫克依库珠单抗治疗,随后单次给予1200毫克治疗。他对该治疗反应迅速,肌酐水平在150微摩尔/升(1.67毫克/分升)左右稳定超过6个月。然而,在最大程度的常规抗蛋白尿治疗下蛋白尿仍未减轻,发病11个月后的重复肾活检显示有严重的慢性改变。我们认为该病例提供了原理证明,即补体抑制在IgAN中可能有益,但慢性病变的发展可能与补体无关。